I've found that you only have to drink about 50% of the mixture at most. Once you start spraying clear liquid you're good.I was kinda surprised that I was completely empty of solids within about an hour of the first dose. Probably didn't even need the second. Maybe they do that to make sure they cover the knuckleheads who forget or just can't do that duration with zero solids. Or people who eat a lot and are constipated? Two definitely seemed like overkill for me and sucked because it meant I was up all night.
Good luck. Hoping all goes well.Prep coming up. But for now after seeing some red and a couple bouts of unexplainable light nausea I'm going to see the gastro on Mon. In 2017 I had an adenoma removed. I was supposed to go back the following year since I wasn't completely cleaned out but put it off.
This is correct. I've been getting a colonoscopy done just about every year since I was 8 (Crohn's disease) and I've never actually finished the prep. Never an issue in my life.Penguin said:I've found that you only have to drink about 50% of the mixture at most. Once you start spraying clear liquid you're good.
I'd look at reviews on any doc. You definitely want good bedside manner for this. If he sucked you can always get your medical records including the photos they take for a second opinion. If you have colon cancer in your immediate family or are high risk I'd rather find someone who is very good. Jmo.How important is finding a good doctor for a colonoscopy? Does it matter that much?
Yeah get it checked out. The good thing if there is anything wrong finding it early has very positive outcomes.I just got my letter. I think it's every two years and I have had four or five over the years. I'm a little nervous as I have been having a lot of pain back there recently. I gotta call it in.
Finding a good doctor for a colonoscopy is a real pain in theHow important is finding a good doctor for a colonoscopy? Does it matter that much?
Well I don’t know about you but........How important is finding a good doctor for?
At 50 you should start. Colon cancer is the only cancer that's totally curable if caught early. If it's in your family, start at 45.Do you need to get a colonoscopy?
What meds are you on? I had ulcerative colitis for 8 years before a total colectomy/rectum removal. Ileostomy for 18 months. 4 surgeries and I now have a Jpouch. I just had my 12th scope in the last 10 years and now they think my internal pouch has Crohn's, covered with ulcers. After the biopsies come in Doc expects to put me on Humira. I've had cipro/flagyl, xifaxan, entecourt all to little or no avail.This is correct. I've been getting a colonoscopy done just about every year since I was 8 (Crohn's disease) and I've never actually finished the prep. Never an issue in my life.![]()
Sorry to hear this brah. I too have colitis. Started humira 3 months ago and got my life back. Hope it works for you too!What meds are you on? I had ulcerative colitis for 8 years before a total colectomy/rectum removal. Ileostomy for 18 months. 4 surgeries and I now have a Jpouch. I just had my 12th scope in the last 10 years and now they think my internal pouch has Crohn's, covered with ulcers. After the biopsies come in Doc expects to put me on Humira. I've had cipro/flagyl, xifaxan, entecourt all to little or no avail.
It all started with a little blood in the stool...chronic autoimmune diseases are not much fun.
Wow yours sounds a lot worse than mine. I was diagnosed when I was 8 (I'm now about to turn 42). For about 15 years, I was pretty much completely in remission. I started to then get a flare up around once a year but prednisone would usually diffuse it pretty quickly. My doctor put me on Humira a couple years ago but that failed after about a year. I'm now on Stalera (and Imuran) and have had no flare ups since. For the most part, the disease doesn't have much of a negative effect on me.What meds are you on? I had ulcerative colitis for 8 years before a total colectomy/rectum removal. Ileostomy for 18 months. 4 surgeries and I now have a Jpouch. I just had my 12th scope in the last 10 years and now they think my internal pouch has Crohn's, covered with ulcers. After the biopsies come in Doc expects to put me on Humira. I've had cipro/flagyl, xifaxan, entecourt all to little or no avail.
It all started with a little blood in the stool...chronic autoimmune diseases are not much fun.
Good luck! I hope it works for you. If it doesn't, there are plenty of other options.Sorry to hear this brah. I too have colitis. Started humira 3 months ago and got my life back. Hope it works for you too!![]()
It sounds worse than it is. I go to the can often but you learn to deal. Prednisone made me a madman, worse than normal. Every time I get a new GI they say, "well, Prednisone is an option".Wow yours sounds a lot worse than mine. I was diagnosed when I was 8 (I'm now about to turn 42). For about 15 years, I was pretty much completely in remission. I started to then get a flare up around once a year but prednisone would usually diffuse it pretty quickly. My doctor put me on Humira a couple years ago but that failed after about a year. I'm now on Stalera (and Imuran) and have had no flare ups since. For the most part, the disease doesn't have much of a negative effect on me.
Wow didn’t realize it could work for a bit then failWow yours sounds a lot worse than mine. I was diagnosed when I was 8 (I'm now about to turn 42). For about 15 years, I was pretty much completely in remission. I started to then get a flare up around once a year but prednisone would usually diffuse it pretty quickly. My doctor put me on Humira a couple years ago but that failed after about a year. I'm now on Stalera (and Imuran) and have had no flare ups since. For the most part, the disease doesn't have much of a negative effect on me.
Prednisone isn't something that you should generally take long term. I use it for 2 weeks at a time to deal with the flare ups. It works great for me. The crazy thing about this disease (and really most diseases) is that every person's ideal treatment course is so different. What works for one person may not work for another. And there is so little data on what are the actual factors that drive personalized treatment choices.It sounds worse than it is. I go to the can often but you learn to deal. Prednisone made me a madman, worse than normal. Every time I get a new GI they say, "well, Prednisone is an option".
I say, "uh no".
Yeah I was on it for about a year and then had a flare up. Now perhaps I could have stayed on it but my doctor decided to switch me to Stalera immediately. Nobody knows what causes these flare ups.Wow didn’t realize it could work for a bit then fail. Did symptoms return and that’s how you knew? Hate this disease.
Thanks Fred for sharing, I think only folks with this disease trusty understand the psychological effect it has on its victims. If I have to switch I may PM you.Yeah I was on it for about a year and then had a flare up. Now perhaps I could have stayed on it but my doctor decided to switch me to Stalera immediately. Nobody knows what causes these flare ups.![]()
Any timeThanks Fred for sharing, I think only folks with this disease trusty understand the psychological effect it has on its victims. If I have to switch I may PM you.
Wow. I'm sitting in the hospital now looking at what's probably gonna be a colectomy/j pouch. I was diagnosed with UC about three weeks ago. I started Remicade, but before it could do anything I developed something called Toxic Megacolon (dibs on the band name) . It's all happened so fast, I don't know what to think. I'm kind of glad that they might just remove it instead of having to take lifelong meds and being on a bunch of dietary restrictions. Maybe I'm crazy for that, but what do you think?What meds are you on? I had ulcerative colitis for 8 years before a total colectomy/rectum removal. Ileostomy for 18 months. 4 surgeries and I now have a Jpouch. I just had my 12th scope in the last 10 years and now they think my internal pouch has Crohn's, covered with ulcers. After the biopsies come in Doc expects to put me on Humira. I've had cipro/flagyl, xifaxan, entecourt all to little or no avail.
It all started with a little blood in the stool...chronic autoimmune diseases are not much fun.
At least you are lucky your colectomy will be a planned surgery. Mine was an emergency when my megacolon blew up. I was rushed in an ambulance and woke up the next day in IC on a respirator, catheter and a new bag on my hip.Wow. I'm sitting in the hospital now looking at what's probably gonna be a colectomy/j pouch. I was diagnosed with UC about three weeks ago. I started Remicade, but before it could do anything I developed something called Toxic Megacolon (dibs on the band name) . It's all happened so fast, I don't know what to think. I'm kind of glad that they might just remove it instead of having to take lifelong meds and being on a bunch of dietary restrictions. Maybe I'm crazy for that, but what do you think?
Good luck bro!I’m on my major prep day. My dad had major surgery recently for an aortic aneurysm, the exact condition and place that killed John Ritter (at age 54.) — my dad is 74. It can be genetic, so scheduled an Ultrasound today for me. Only problem is I haven’t been able to eat or drink anything since ten last night and can’t until noon. So on top of the liquids only (and jello) today, the first half of my day I’m empty and bone dry. Even so, feel good and will make up for lost time with water, bone broth, jello and Italian ice as soon as I’m done with the Ultrasound. T-minus 6 hours or so until I commence crap rocket protocol. In a perverse sort of way, I’m looking forward to the experience and the post Colonoscopy meal tomorrow.
Evacuate the family from your house! Pun intended!Two Ducolax and 45 mins later some serious rumbly in my tumbly, followed by a deep alto toot. 15 mins until I drink the witches brew.
The magic elixir that keeps on giving!!!Hour fifteen since I finished 34 ounces. Been some rumbles, but no sign of impending calamity. Any guidance on when I can expect events?
Edit: Answer was fifteen minutes later.
Then 10 minutes later.
You don't want to hear those terrible words I heard. You aren't completely cleaned out. You need to redo it.Slept for four hours and decided to go with the second load of concoction. I can see where other posters said it is close enough after one load, but I can also see why they might recommend the second.
If it's actually diverticulitis maybe ask about antibiotics. When I had mild diverticulitis they put me on antibiotics. Then the diagnosis becomes diverticulosis which is always there but harmless. Just need to fiber up more.Have mild diverticulitis, which is common. Half of people by 60 (I’m 48.) tracks because I did high protein low carb diets for years, and is consistent with low fiber diets. I’ve improved diet over last couple years — though overall very healthy.
No polyps. 10 years until next one.
Overall, ain’t no thing. Woke up feeling craze amaze from the propofol (45 mins ago.) More or less fine now. Barely groggy.
Seen this?This is correct. I've been getting a colonoscopy done just about every year since I was 8 (Crohn's disease) and I've never actually finished the prep. Never an issue in my life.![]()
That sounds absolutely gross! And yet surprisingly wonderful at the same time!Seen this?
Besides making for the easiest jokes ever, it looks like there's real hope for your condition. I.e. it's the good ####.
I'll pay extra for the candy coating on that oneSeen this?
Besides making for the easiest jokes ever, it looks like there's real hope for your condition. I.e. it's the good ####.
I have my first colonscopy this Thursday (yay - i'm old!). Had COVID test this morning (nostril). wasn't too bad.Looking for a little insight from those that have had a colonoscopy. I have been having lingering abdominal pains for several months. I spoke with a GI specialist on Friday and she has scheduled me for a colonoscopy as well as an endoscopy. I am 51 and never had a colonoscopy, so I was due to have the procedure. I am curious what to expect in the days leading up to the procedure as well as what I need to do to prepare for this procedure?
For me, if I make it through the prep I'M 90% there. I struggle with the taste. The procedure itself it pretty easy as they put you out and all that. Some have bloating and a bunch of gas after. The meal after is heaven.Looking for a little insight from those that have had a colonoscopy. I have been having lingering abdominal pains for several months. I spoke with a GI specialist on Friday and she has scheduled me for a colonoscopy as well as an endoscopy. I am 51 and never had a colonoscopy, so I was due to have the procedure. I am curious what to expect in the days leading up to the procedure as well as what I need to do to prepare for this procedure?
Just make sure you do the prep properly and exactly as they prescribe it.Looking for a little insight from those that have had a colonoscopy. I have been having lingering abdominal pains for several months. I spoke with a GI specialist on Friday and she has scheduled me for a colonoscopy as well as an endoscopy. I am 51 and never had a colonoscopy, so I was due to have the procedure. I am curious what to expect in the days leading up to the procedure as well as what I need to do to prepare for this procedure?
Having mine on dec 8.I have my first colonscopy this Thursday (yay - i'm old!). Had COVID test this morning (nostril). wasn't too bad.
I haven't had issues with the prep but this is pretty spot on.For me, if I make it through the prep I'M 90% there. I struggle with the taste. The procedure itself it pretty easy as they put you out and all that. Some have bloating and a bunch of gas after. The meal after is heaven.
Yeah. Butt if you can squeeze another day off, doodoo it.Thanks for the input everyone. Were you guys back at work the day after the procedure? Tryign to give my boss a heads-up.
I see what you did there.Yeah. Butt if you can squeeze another day off, doodoo it.
Had one a year ago. It really was nothing. The prep was the "scariest" as you hear stories and think the worst. I started the prep at like 2 pm or something. Had to take a stool softener. Then at like 6 I had to start drinking the mix. 8 ounces every 15 minutes or something like that. I just played video games and waited. Once I was almost completely done with drinking all the mix, I started to worry because things hadn't started working. Then it hit me. Went and basically peed out my butt a couple of times. Unlike being sick and having the runs, there was NO cramping. Was kind of weird. Next day, went in and they were getting me ready for the procedure. The last thing I remember was telling the nurse who had just administered the IV shot to put me in la-la land "Hey, I'm a big dude. You may need to double that up". She laughed at me and the next thing I knew I was in recovery. Had a bit of gas. That felt weird just ripping them off in the recovery room but they reassured me that it was "normal".Looking for a little insight from those that have had a colonoscopy. I have been having lingering abdominal pains for several months. I spoke with a GI specialist on Friday and she has scheduled me for a colonoscopy as well as an endoscopy. I am 51 and never had a colonoscopy, so I was due to have the procedure. I am curious what to expect in the days leading up to the procedure as well as what I need to do to prepare for this procedure?
This is great info.I haven't had issues with the prep but this is pretty spot on.
My hint is to try to schedule for early morning. You do your prep the afternoon before and you're sleeping with empty stomach. Only issue then is you can't drink anything in morning but better than doing it later in day.
They knock you out and then you wake up in post-op waiting to go home for lunch.